IL179730A0 - Novel cis-imidazolines - Google Patents
Novel cis-imidazolinesInfo
- Publication number
- IL179730A0 IL179730A0 IL179730A IL17973006A IL179730A0 IL 179730 A0 IL179730 A0 IL 179730A0 IL 179730 A IL179730 A IL 179730A IL 17973006 A IL17973006 A IL 17973006A IL 179730 A0 IL179730 A0 IL 179730A0
- Authority
- IL
- Israel
- Prior art keywords
- imidazolines
- novel cis
- cis
- novel
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/20—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D233/22—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US58044104P | 2004-06-17 | 2004-06-17 | |
US67419605P | 2005-04-22 | 2005-04-22 | |
PCT/EP2005/006167 WO2005123691A1 (en) | 2004-06-17 | 2005-06-08 | Novel cis-imidazolines |
Publications (1)
Publication Number | Publication Date |
---|---|
IL179730A0 true IL179730A0 (en) | 2007-05-15 |
Family
ID=34969621
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL179730A IL179730A0 (en) | 2004-06-17 | 2006-11-30 | Novel cis-imidazolines |
Country Status (16)
Country | Link |
---|---|
US (1) | US7893278B2 (en) |
EP (1) | EP1758868A1 (en) |
JP (1) | JP4809336B2 (en) |
KR (1) | KR100855929B1 (en) |
AR (1) | AR049647A1 (en) |
AU (1) | AU2005254643A1 (en) |
BR (1) | BRPI0512237A (en) |
CA (1) | CA2569598A1 (en) |
IL (1) | IL179730A0 (en) |
MX (1) | MXPA06014806A (en) |
NO (1) | NO20070295L (en) |
NZ (1) | NZ551659A (en) |
RU (1) | RU2408593C2 (en) |
SG (1) | SG148177A1 (en) |
TW (1) | TW200637828A (en) |
WO (1) | WO2005123691A1 (en) |
Families Citing this family (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2006224765B2 (en) | 2005-03-16 | 2012-02-09 | F.Hoffmann-La Roche Ag | CIS-2,4,5-triaryl-imidazolines and their use as anti-cancer medicaments |
EP2130822A1 (en) | 2005-12-01 | 2009-12-09 | F. Hoffmann-La Roche AG | 2,4,5-triphenyl imidazoline derivatives as inhibitors of the interaction between p53 and mdm2 proteins for use as anticancer agents |
EP1979338A1 (en) * | 2006-01-18 | 2008-10-15 | F.Hoffmann-La Roche Ag | Cis-4, 5-biaryl-2-heterocyclic-imidazolines as mdm2 inhibitors |
CN101605798A (en) | 2006-12-14 | 2009-12-16 | 第一三共株式会社 | Imidazothiazole derivative |
PT2118123E (en) * | 2007-01-31 | 2016-02-10 | Harvard College | Stabilized p53 peptides and uses thereof |
ES2430067T3 (en) | 2007-03-28 | 2013-11-18 | President And Fellows Of Harvard College | Sewn polypeptides |
US7625895B2 (en) * | 2007-04-12 | 2009-12-01 | Hoffmann-Le Roche Inc. | Diphenyl-dihydro-imidazopyridinones |
WO2008144614A1 (en) * | 2007-05-21 | 2008-11-27 | Lubrizol Advanced Materials, Inc. | Polyurethane polymer |
EP2249832A4 (en) * | 2008-01-30 | 2011-12-21 | Agency Science Tech & Res | Method for treating fibrosis and cancer with imidazolium and imidazolinium compounds |
EP2271338A4 (en) * | 2008-03-31 | 2011-05-04 | Agency Science Tech & Res | Method for treating neurological disorders with imidazolium and imidazolinium compounds |
EP2298778A4 (en) | 2008-06-12 | 2011-10-05 | Daiichi Sankyo Co Ltd | Imidazothiazole derivative having 4,7-diazaspiroý2.5¨octane ring structure |
ES2463820T3 (en) | 2009-01-16 | 2014-05-29 | Daiichi Sankyo Company, Limited | Imidazothiazole derivative that has a proline ring structure |
JO2998B1 (en) | 2010-06-04 | 2016-09-05 | Amgen Inc | Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer |
US8889863B2 (en) | 2010-07-16 | 2014-11-18 | Vanderbilt University | Stereoselective methods, catalysts and intermediates for the synthesis of (−)-Nutlin-3 and related compounds |
KR20180058866A (en) | 2010-08-13 | 2018-06-01 | 에일러론 테라퓨틱스 인코포레이티드 | Peptidomimetic macrocycles |
EP2621275B1 (en) | 2010-09-30 | 2018-03-28 | St. Jude Children's Research Hospital | Aryl-substituted imidazoles |
MX352672B (en) | 2011-09-27 | 2017-12-04 | Amgen Inc | Heterocyclic compounds as mdm2 inhibitors for the treatment of cancer. |
BR112014009418A2 (en) | 2011-10-18 | 2017-04-18 | Aileron Therapeutics Inc | peptidomimetic macrocycles |
US8927500B2 (en) | 2012-02-15 | 2015-01-06 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles |
US8987414B2 (en) | 2012-02-15 | 2015-03-24 | Aileron Therapeutics, Inc. | Triazole-crosslinked and thioether-crosslinked peptidomimetic macrocycles |
JP6526563B2 (en) | 2012-11-01 | 2019-06-05 | エイルロン セラピューティクス,インコーポレイテッド | Disubstituted amino acids and methods for their preparation and use |
BR112015013611A2 (en) | 2012-12-20 | 2017-11-14 | Merck Sharp & Dohme | compound and pharmaceutical composition |
US11407721B2 (en) | 2013-02-19 | 2022-08-09 | Amgen Inc. | CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer |
WO2014134201A1 (en) | 2013-02-28 | 2014-09-04 | Amgen Inc. | A benzoic acid derivative mdm2 inhibitor for the treatment of cancer |
CA2906538C (en) | 2013-03-14 | 2021-02-02 | Ana Gonzalez Buenrostro | Heteroaryl acid morpholinone compounds as mdm2 inhibitors for the treatment of cancer |
ES2875853T3 (en) | 2013-03-15 | 2021-11-11 | Univ Texas | Method of treating fibrosis |
JOP20200296A1 (en) | 2013-06-10 | 2017-06-16 | Amgen Inc | Processes of Making and Crystalline Forms of a MDM2 Inhibitor |
WO2015116735A1 (en) | 2014-01-28 | 2015-08-06 | Mayo Foundation For Medical Education And Research | Methods and combinations for killing senescent cells and for treating senescence-associated diseases and disorders |
US10328058B2 (en) | 2014-01-28 | 2019-06-25 | Mayo Foundation For Medical Education And Research | Treating atherosclerosis by removing senescent foam cell macrophages from atherosclerotic plaques |
JP6688224B2 (en) | 2014-01-28 | 2020-04-28 | バック インスティテュート フォー リサーチ オン エイジング | Treatment of osteoarthritis in joints by administration of means that inhibit MDM2 |
JP2017533889A (en) | 2014-09-24 | 2017-11-16 | エルロン・セラピューティクス・インコーポレイテッドAileron Therapeutics,Inc. | Peptidomimetic macrocycles and uses thereof |
CN107106642B (en) | 2014-09-24 | 2021-02-26 | 艾瑞朗医疗公司 | Peptidomimetic macrocycles and formulations thereof |
CA2979847A1 (en) | 2015-03-20 | 2016-09-29 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles and uses thereof |
CN108368161A (en) | 2015-09-10 | 2018-08-03 | 艾瑞朗医疗公司 | Peptidomimetic macrocyclic compound as MCL-1 conditioning agents |
EP3429570A1 (en) | 2016-03-15 | 2019-01-23 | Oryzon Genomics, S.A. | Combinations of lsd1 inhibitors for the treatment of hematological malignancies |
EP3429571A1 (en) | 2016-03-15 | 2019-01-23 | Oryzon Genomics, S.A. | Combinations of lsd1 inhibitors for use in the treatment of solid tumors |
PL3458101T3 (en) | 2016-05-20 | 2021-05-31 | F. Hoffmann-La Roche Ag | Protac antibody conjugates and methods of use |
CA3033850C (en) | 2017-06-16 | 2020-02-11 | Unity Biotechnology, Inc. | Synthesis method for producing enantiomerically pure cis-imidazoline compounds for pharmaceutical use |
US10588916B2 (en) | 2017-10-31 | 2020-03-17 | Unity Biotechnology, Inc. | Technology to inhibit vascular changes that lead to vision loss in the eye |
JP7204391B2 (en) * | 2018-09-18 | 2023-01-16 | 株式会社東芝 | Acid gas absorbent, method for removing acid gas, and apparatus for removing acid gas |
KR102622992B1 (en) * | 2021-03-29 | 2024-01-10 | 주식회사 퓨전바이오텍 | Method for preparing imidazoline derivatives and intermediates thereof |
WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2441498A (en) * | 1943-07-15 | 1948-05-11 | Astra Apotekarnes Kem Fab | Alkyl glycinanilides |
JPH02101065A (en) | 1988-10-06 | 1990-04-12 | Tanabe Seiyaku Co Ltd | Imidazoline derivative |
DE4203547A1 (en) | 1992-02-07 | 1993-08-12 | Knoll Ag | METHOD FOR RACEMAT SEPARATION OF VERAPAMIL |
GB2351082A (en) | 1999-06-18 | 2000-12-20 | Lilly Forschung Gmbh | Synthesis of Cyclic Substituted Amidines |
US6653501B2 (en) | 2001-06-27 | 2003-11-25 | Napro Biotherapeutics, Inc. | Chiral resolution method for producing compounds useful in the synthesis of taxanes |
ATE389400T1 (en) * | 2001-12-18 | 2008-04-15 | Hoffmann La Roche | CIS-2,4,5-TRIPHENYL-IMIDAZOLINE AND THEIR USE IN THE TREATMENT OF TUMORS |
JP4361798B2 (en) * | 2001-12-18 | 2009-11-11 | エフ.ホフマン−ラ ロシュ アーゲー | Cis-imidazoline as an MDM2 inhibitor |
ES2314660T3 (en) * | 2004-05-18 | 2009-03-16 | F. Hoffmann-La Roche Ag | NEW CIS-IMIDAZOLINAS. |
-
2005
- 2005-06-02 US US11/143,161 patent/US7893278B2/en not_active Expired - Fee Related
- 2005-06-08 WO PCT/EP2005/006167 patent/WO2005123691A1/en active Application Filing
- 2005-06-08 RU RU2007101275/04A patent/RU2408593C2/en not_active IP Right Cessation
- 2005-06-08 KR KR1020067026563A patent/KR100855929B1/en not_active IP Right Cessation
- 2005-06-08 EP EP05750351A patent/EP1758868A1/en not_active Withdrawn
- 2005-06-08 MX MXPA06014806A patent/MXPA06014806A/en active IP Right Grant
- 2005-06-08 AU AU2005254643A patent/AU2005254643A1/en not_active Abandoned
- 2005-06-08 CA CA002569598A patent/CA2569598A1/en not_active Abandoned
- 2005-06-08 BR BRPI0512237-6A patent/BRPI0512237A/en not_active IP Right Cessation
- 2005-06-08 NZ NZ551659A patent/NZ551659A/en unknown
- 2005-06-08 JP JP2007515829A patent/JP4809336B2/en not_active Expired - Fee Related
- 2005-06-08 SG SG200808461-8A patent/SG148177A1/en unknown
- 2005-06-15 AR ARP050102451A patent/AR049647A1/en not_active Application Discontinuation
- 2005-07-08 TW TW094119846A patent/TW200637828A/en unknown
-
2006
- 2006-11-30 IL IL179730A patent/IL179730A0/en unknown
-
2007
- 2007-01-16 NO NO20070295A patent/NO20070295L/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
KR20070027590A (en) | 2007-03-09 |
JP2008502620A (en) | 2008-01-31 |
US20050282803A1 (en) | 2005-12-22 |
RU2408593C2 (en) | 2011-01-10 |
EP1758868A1 (en) | 2007-03-07 |
AU2005254643A1 (en) | 2005-12-29 |
US7893278B2 (en) | 2011-02-22 |
KR100855929B1 (en) | 2008-09-02 |
NZ551659A (en) | 2010-08-27 |
CA2569598A1 (en) | 2005-12-29 |
AR049647A1 (en) | 2006-08-23 |
BRPI0512237A (en) | 2008-02-19 |
SG148177A1 (en) | 2008-12-31 |
RU2007101275A (en) | 2008-07-27 |
WO2005123691A1 (en) | 2005-12-29 |
MXPA06014806A (en) | 2007-02-12 |
NO20070295L (en) | 2007-01-17 |
TW200637828A (en) | 2006-11-01 |
JP4809336B2 (en) | 2011-11-09 |
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